Venkataramana M, Chandra Nayaka S, Anand T, Rajesh Rajaiah, Aiyaz Mohammed, Divakara S T, Murali H S, Prakash H S, Lakshmana Rao P V
DRDO-BU Centre for Life Sciences, Coimbatore, Tamilnadu 641046, India.
DOS in Biotechnology, University of Mysore, Mysore 570006, Karnataka, India.
Food Chem Toxicol. 2014 Mar;65:335-42. doi: 10.1016/j.fct.2013.12.042. Epub 2014 Jan 8.
Zearalenone (ZEN) is a mycotoxin from Fusarium species commonly found in many food commodities and are known to cause reproductive disorders, genotoxic and immunosuppressive effects. Although many studies have demonstrated the cytotoxic effects of ZEN, the mechanisms by which ZEN mediates its cytotoxic effects appear to differ according to cell type and route of exposure. Meantime, the available information on the neurotoxic effects of ZEN is very much limited. In the present study we evaluated the role of oxidative stress in ZEN mediated neurotoxicity in SH-SY5Y cells and investigated the possible underlying mechanism. ZEN induced ROS formation and elevated levels of MDA, loss of mitochondrial membrane potential (MMP) and increase in DNA damage in a dose dependent manner as assessed by COMET assay and agarose gel electrophoresis. However, there was no DNA damage by plasmid breakage assay at 6, 12 and 24h time points. DAPI staining showed apoptotic nuclei at 12 and 24h. Further, ZEN treated SH-SY5Y cells showed a marked suppressive effect on the neuronal gene expression. Use of an antioxidant N-acetylcysteine (NAC) reversed the toxin-induced generation of ROS and also attenuated loss of MMP. Collectively, these results suggest that ROS is the main upstream signal leading to increased ZEN mediated neurotoxicity in SH-SY5Y cells.
玉米赤霉烯酮(ZEN)是一种由镰刀菌属产生的霉菌毒素,常见于许多食品中,已知会导致生殖紊乱、遗传毒性和免疫抑制作用。尽管许多研究已经证明了ZEN的细胞毒性作用,但ZEN介导其细胞毒性作用的机制似乎因细胞类型和暴露途径而异。与此同时,关于ZEN神经毒性作用的现有信息非常有限。在本研究中,我们评估了氧化应激在ZEN介导的SH-SY5Y细胞神经毒性中的作用,并研究了可能的潜在机制。通过彗星试验和琼脂糖凝胶电泳评估,ZEN以剂量依赖性方式诱导活性氧(ROS)形成、丙二醛(MDA)水平升高、线粒体膜电位(MMP)丧失和DNA损伤增加。然而,在6、12和24小时时间点通过质粒断裂试验未发现DNA损伤。DAPI染色显示在12和24小时出现凋亡细胞核。此外,ZEN处理的SH-SY5Y细胞对神经元基因表达表现出显著的抑制作用。使用抗氧化剂N-乙酰半胱氨酸(NAC)可逆转毒素诱导的ROS生成,并减轻MMP的丧失。总体而言,这些结果表明ROS是导致ZEN介导的SH-SY5Y细胞神经毒性增加的主要上游信号。